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HBA1 Antikörper

Dieses Anti-HBA1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von HBA1 in WB, IHC und ELISA. Geeignet für Maus und Ratte.
Produktnummer ABIN7114938

Kurzübersicht für HBA1 Antikörper (ABIN7114938)

Target

Alle HBA1 Antikörper anzeigen
HBA1 (Hemoglobin, alpha 1 (HBA1))

Reaktivität

  • 40
  • 19
  • 3
  • 3
  • 2
Maus, Ratte

Wirt

  • 45
  • 8
Kaninchen

Klonalität

  • 43
  • 10
Polyklonal

Konjugat

  • 32
  • 7
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser HBA1 Antikörper ist unkonjugiert

Applikation

  • 38
  • 23
  • 16
  • 12
  • 10
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Aufreinigung

    Immunogen affinity purified

    Reinheit

    ≥95 % as determined by SDS-PAGE

    Immunogen

    hemoglobin, alpha 1

    Isotyp

    IgG
  • Applikationshinweise

    WB: 1:500 - 1:2000, IHC: 1:50 - 1:100

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    -20°C for 12 months (Avoid repeated freeze / thaw cycles.)

    Haltbarkeit

    12 months
  • Target

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    Andere Bezeichnung

    Hemoglobin alpha

    Hintergrund

    Synonyms:Alpha globin, HBA1, HBA2, Hemoglobin a, Hemoglobin alpha chain, Hemoglobin subunit alpha, hemoglobin, alpha 1 Background:The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. The alpha-2 (HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin; alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1; some nondeletion alpha thalassemias have also been reported.

    Molekulargewicht

    13 kDa

    Gen-ID

    3040

    UniProt

    P69905
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